ClinGen Allele Registry
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Canonical Allele Identifier:
CA15233077
Gene: ADAMTS9-AS2
HGNC
NCBI
Linked Data
dbSNP Id:
rs2371767
gnomAD v2:
3-64718258-G-C
gnomAD v3:
3-64732582-G-C
gnomAD v4:
3-64732582-G-C
MyVariant Identifiers:
chr3:g.64718258G>C (hg19)
chr3:g.64732582G>C (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.64732582G>C , CM000665.2:g.64732582G>C
GRCh38
NC_000003.11:g.64718258G>C , CM000665.1:g.64718258G>C
GRCh37
NC_000003.10:g.64693298G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_038264.1:n.469+47244G>C
Search 100 bp 5'
Search 100 bp 3'